A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714940



Internal ID19013221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19476237..19586414hg38UCSC Ensembl
Innerchr13:20050377..20160554hg19UCSC Ensembl
Innerchr13:18948377..19058554hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38110178
hg19110178
hg18110178
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046064
Supporting Variants
Samples
Known GenesTPTE2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3714940
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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